CA3065951A1 - Anticorps uniquement a chaines lourdes anti-bcma - Google Patents
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- CA3065951A1 CA3065951A1 CA3065951A CA3065951A CA3065951A1 CA 3065951 A1 CA3065951 A1 CA 3065951A1 CA 3065951 A CA3065951 A CA 3065951A CA 3065951 A CA3065951 A CA 3065951A CA 3065951 A1 CA3065951 A1 CA 3065951A1
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- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2878—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C—CHEMISTRY; METALLURGY
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- C07K—PEPTIDES
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- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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- C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
- C07K16/2809—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against the T-cell receptor (TcR)-CD3 complex
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- A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
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- C—CHEMISTRY; METALLURGY
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
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- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
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- C—CHEMISTRY; METALLURGY
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- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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- C—CHEMISTRY; METALLURGY
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- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
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- C—CHEMISTRY; METALLURGY
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- C—CHEMISTRY; METALLURGY
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- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
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- Medicinal Chemistry (AREA)
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- Veterinary Medicine (AREA)
- Peptides Or Proteins (AREA)
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- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
L'invention concerne des anticorps uniquement à chaînes lourdes anti-BCMA (HCAb) et des procédés de préparation de tels anticorps, des compositions, y compris des compositions pharmaceutiques, comprenant de tels anticorps, et leur utilisation pour traiter des troubles de lymphocytes B caractérisés par l'expression de BCMA.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762522295P | 2017-06-20 | 2017-06-20 | |
| US62/522,295 | 2017-06-20 | ||
| PCT/US2018/038506 WO2018237006A1 (fr) | 2017-06-20 | 2018-06-20 | Anticorps uniquement à chaînes lourdes anti-bcma |
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| AU (1) | AU2018288803A1 (fr) |
| BR (1) | BR112019026803A2 (fr) |
| CA (1) | CA3065951A1 (fr) |
| MX (1) | MX2019015563A (fr) |
| WO (1) | WO2018237006A1 (fr) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3029209A1 (fr) | 2016-06-21 | 2017-12-28 | Teneobio, Inc. | Anticorps se liant a cd3 |
| BR112019004873A2 (pt) | 2016-09-14 | 2019-06-11 | Teneobio Inc | anticorpos de ligação a cd3 |
| MX2019007379A (es) | 2016-12-21 | 2019-09-18 | Teneobio Inc | Anticuerpos anti-bcma unicamente de cadena pesada. |
| CN117866097A (zh) * | 2017-06-20 | 2024-04-12 | 特尼奥生物股份有限公司 | 仅有重链的抗bcma抗体 |
| JP7240335B2 (ja) | 2017-06-20 | 2023-03-15 | テネオワン， インコーポレイテッド | 抗ｂｃｍａ重鎖のみ抗体 |
| EP3728319A1 (fr) | 2017-12-22 | 2020-10-28 | TeneoBio, Inc. | Anticorps à chaîne lourde se liant à cd22 |
| BR112020024351A2 (pt) | 2018-06-01 | 2021-02-23 | Novartis Ag | moléculas de ligação contra bcma e usos das mesmas |
| WO2020252366A1 (fr) | 2019-06-14 | 2020-12-17 | Teneobio, Inc. | Anticorps à chaînes lourdes multispécifiques se liant à cd22 et cd3 |
| CN112574308A (zh) * | 2019-09-30 | 2021-03-30 | 和铂医药(苏州)有限公司 | 靶向bcma的抗体、双特异性抗体及其用途 |
| WO2021222578A1 (fr) | 2020-04-29 | 2021-11-04 | Teneobio, Inc. | Anticorps à chaîne lourde multispécifiques ayant des régions constantes de chaîne lourde modifiées |
| US20230203161A1 (en) | 2020-04-29 | 2023-06-29 | Teneobio, Inc | Multispecific heavy chain antibodies with modified heavy chain constant regions |
| EP4171750A1 (fr) * | 2020-06-30 | 2023-05-03 | Teneobio, Inc. | Anticorps multi-spécifiques se liant à bcma |
| TW202330612A (zh) * | 2021-10-20 | 2023-08-01 | 日商武田藥品工業股份有限公司 | 靶向ｂｃｍａ之組合物及其使用方法 |
Family Cites Families (94)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| CA1288073C (fr) | 1985-03-07 | 1991-08-27 | Paul G. Ahlquist | Vecteur de transformation de l'arn |
| IL85035A0 (en) | 1987-01-08 | 1988-06-30 | Int Genetic Eng | Polynucleotide molecule,a chimeric antibody with specificity for human b cell surface antigen,a process for the preparation and methods utilizing the same |
| GB8928874D0 (en) | 1989-12-21 | 1990-02-28 | Celltech Ltd | Humanised antibodies |
| US6750325B1 (en) | 1989-12-21 | 2004-06-15 | Celltech R&D Limited | CD3 specific recombinant antibody |
| US5968509A (en) | 1990-10-05 | 1999-10-19 | Btp International Limited | Antibodies with binding affinity for the CD3 antigen |
| US6407213B1 (en) | 1991-06-14 | 2002-06-18 | Genentech, Inc. | Method for making humanized antibodies |
| GB9206422D0 (en) | 1992-03-24 | 1992-05-06 | Bolt Sarah L | Antibody preparation |
| US7381803B1 (en) | 1992-03-27 | 2008-06-03 | Pdl Biopharma, Inc. | Humanized antibodies against CD3 |
| US5731168A (en) | 1995-03-01 | 1998-03-24 | Genentech, Inc. | Method for making heteromultimeric polypeptides |
| US6096871A (en) | 1995-04-14 | 2000-08-01 | Genentech, Inc. | Polypeptides altered to contain an epitope from the Fc region of an IgG molecule for increased half-life |
| EP0904107B1 (fr) | 1996-03-18 | 2004-10-20 | Board Of Regents, The University Of Texas System | Domaines analogues a l'immunoglobuline a demi-vies prolongees |
| IL132560A0 (en) | 1997-05-02 | 2001-03-19 | Genentech Inc | A method for making multispecific antibodies having heteromultimeric and common components |
| JP4253826B2 (ja) | 1999-09-07 | 2009-04-15 | カシオ計算機株式会社 | 画像読取装置 |
| UA74798C2 (uk) | 1999-10-06 | 2006-02-15 | Байоджен Айдек Ма Інк. | Спосіб лікування раку у ссавця за допомогою поліпептиду, що протидіє взаємодії april з його рецепторами |
| WO2001024812A1 (fr) | 1999-10-06 | 2001-04-12 | N.V. Nutricia | UTILISATION DU FACTEUR DE CROISSANCE TRANSFORMANT β ET DE FACTEURS DE CROISSANCE POUR LE TRAITEMENT ET LA PREVENTION D'UNE MALADIE DE LA MUQUEUSE INTESTINALE |
| AU2002238052A1 (en) | 2001-02-20 | 2002-09-04 | Zymogenetics, Inc. | Antibodies that bind both bcma and taci |
| CN1195779C (zh) | 2001-05-24 | 2005-04-06 | 中国科学院遗传与发育生物学研究所 | 抗人卵巢癌抗人cd3双特异性抗体 |
| GB0115256D0 (en) | 2001-06-21 | 2001-08-15 | Babraham Inst | Mouse light chain locus |
| AU2003287345A1 (en) | 2002-10-31 | 2004-06-07 | Genentech, Inc. | Methods and compositions for increasing antibody production |
| AU2004205684A1 (en) | 2003-01-23 | 2004-08-05 | Genentech, Inc. | Methods for producing humanized antibodies and improving yield of antibodies or antigen binding fragments in cell culture |
| EP1629012B1 (fr) | 2003-05-31 | 2018-11-28 | Amgen Research (Munich) GmbH | Compositions pharmaceutiques comprenant des constructions d'anticorps anti-cd3, anti-cd19 bispecifiques pour le traitement de troubles associes aux lymphocytes b |
| EA010350B1 (ru) | 2004-06-03 | 2008-08-29 | Новиммун С.А. | Антитела против cd3 и способы их применения |
| RU2398882C2 (ru) | 2004-07-22 | 2010-09-10 | Эрасмус Юниверсити Медикал Сентр Роттердам | СПОСОБ ПОЛУЧЕНИЯ АНТИГЕН-СВЯЗЫВАЮЩЕГО ДОМЕНА Vh ИСПОЛЬЗОВАНИЕ |
| RU2492186C2 (ru) | 2005-02-18 | 2013-09-10 | Медарекс Ллс | Выделенное анти-cd30 антитело (варианты), хозяйская клетка, способ получения химерного или гуманизированного варианта анти-cd30 антител (варианты), способ ингибирования роста клеток cd30+ и способ ингибирования роста опухолевых клеток, экспрессирующих cd30 |
| US20160355591A1 (en) | 2011-05-02 | 2016-12-08 | Immunomedics, Inc. | Subcutaneous anti-hla-dr monoclonal antibody for treatment of hematologic malignancies |
| US7612181B2 (en) | 2005-08-19 | 2009-11-03 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
| EP2354162A1 (fr) | 2005-09-12 | 2011-08-10 | Novimmune SA | Formulations d'anticorps anti-CD3 |
| JP5686953B2 (ja) | 2005-10-11 | 2015-03-18 | アムゲン リサーチ （ミュンヘン） ゲーエムベーハー | 交差種特異的（ｃｒｏｓｓ−ｓｐｅｃｉｅｓ−ｓｐｅｃｉｆｉｃ）抗体を含む組成物および該組成物の使用 |
| CN101426815A (zh) | 2005-12-06 | 2009-05-06 | 杜门蒂斯有限公司 | 具有表皮生长因子受体和/或血管内皮生长因子结合特异性的配体及其使用方法 |
| WO2007117600A2 (fr) | 2006-04-07 | 2007-10-18 | Macrogenics, Inc. | Polythérapie pour le traitement de maladies autoimmunes |
| WO2008016431A2 (fr) | 2006-07-29 | 2008-02-07 | Robert Lamar Bjork | Médicament thérapeutique d'anticorps monoclonal bispécifique ( spécifique à la fois à cd3 et cd11b) |
| NZ580755A (en) | 2007-04-03 | 2012-05-25 | Micromet Ag | Cross-species-specific cd3-epsilon binding domain |
| WO2008151081A1 (fr) | 2007-06-01 | 2008-12-11 | Omt, Inc. | Compositions et procédés pour inhiber des gènes d'immunoglobuline endogènes et produire des anticorps d'idiotype humains transgéniques |
| WO2009030285A1 (fr) | 2007-09-07 | 2009-03-12 | Ablynx N.V. | Molécules de liaison présentant plusieurs sites de liaison, compositions comprenant de telles molécules et utilisations de celles-ci |
| CA2720682A1 (fr) | 2008-04-25 | 2009-10-29 | Zymogenetics, Inc. | Niveaux d'expression de la proteine bcma sur les lymphocytes b et utilisation dans de methodes diagnostiques |
| US20100122358A1 (en) | 2008-06-06 | 2010-05-13 | Crescendo Biologics Limited | H-Chain-only antibodies |
| SI2356153T1 (sl) | 2008-10-01 | 2016-07-29 | Amgen Research (Munich) Gmbh | Bispecifično enoverižno protitelo, specifično za križane vrste |
| PT2406284T (pt) | 2009-03-10 | 2016-09-29 | Biogen Ma Inc | Anticorpos anti-bcma |
| GB0905023D0 (en) | 2009-03-24 | 2009-05-06 | Univ Erasmus Medical Ct | Binding molecules |
| US9345661B2 (en) | 2009-07-31 | 2016-05-24 | Genentech, Inc. | Subcutaneous anti-HER2 antibody formulations and uses thereof |
| ES2547142T5 (es) | 2010-02-08 | 2021-12-09 | Regeneron Pharma | Cadena ligera común de ratón |
| TWI653333B (zh) | 2010-04-01 | 2019-03-11 | 安進研究（慕尼黑）有限責任公司 | 跨物種專一性之ＰＳＭＡｘＣＤ３雙專一性單鏈抗體 |
| US20130273055A1 (en) | 2010-11-16 | 2013-10-17 | Eric Borges | Agents and methods for treating diseases that correlate with bcma expression |
| WO2012122512A1 (fr) | 2011-03-10 | 2012-09-13 | Hco Antibody, Inc. | Production recombinante de mélanges d'anticorps monocaténaires |
| US20130101599A1 (en) | 2011-04-21 | 2013-04-25 | Boehringer Ingelheim International Gmbh | Bcma-based stratification and therapy for multiple myeloma patients |
| LT3415531T (lt) | 2011-05-27 | 2023-09-25 | Glaxo Group Limited | Bcma (cd269/tnfrsf17) – surišantys baltymai |
| TWI679212B (zh) | 2011-11-15 | 2019-12-11 | 美商安進股份有限公司 | 針對ｂｃｍａ之e3以及ｃｄ３的結合分子 |
| RU2673153C2 (ru) | 2012-04-20 | 2018-11-22 | АПТЕВО РИСЁРЧ ЭНД ДИВЕЛОПМЕНТ ЭлЭлСи | Полипептиды, связывающиеся с cd3 |
| US20150203591A1 (en) | 2012-08-02 | 2015-07-23 | Regeneron Pharmaceuticals, Inc. | Mutivalent antigen-binding proteins |
| JOP20200236A1 (ar) | 2012-09-21 | 2017-06-16 | Regeneron Pharma | الأجسام المضادة لمضاد cd3 وجزيئات ربط الأنتيجين ثنائية التحديد التي تربط cd3 وcd20 واستخداماتها |
| US10189906B2 (en) * | 2012-11-01 | 2019-01-29 | Max-Delrück-Centrum Für Molekulare Medizin | Antibody that binds CD269 (BCMA) suitable for use in the treatment of plasma cell diseases such as multiple myeloma and autoimmune diseases |
| TW201425336A (zh) * | 2012-12-07 | 2014-07-01 | Amgen Inc | Ｂｃｍａ抗原結合蛋白質 |
| KR102239125B1 (ko) | 2012-12-14 | 2021-04-12 | 오픈 모노클로날 테크놀로지, 인코포레이티드 | 인간 이디오타입을 갖는 설치류 항체를 인코딩하는 폴리뉴클레오티드 및 이를 포함하는 동물 |
| EP2953972B1 (fr) | 2013-02-05 | 2020-07-08 | EngMab Sàrl | Procédé pour la sélection d'anticorps contre bcma |
| TN2016000142A1 (en) | 2013-10-31 | 2017-10-06 | Sanofi Sa | Specific anti-cd38 antibodies for treating human cancers. |
| NZ720161A (en) | 2013-11-04 | 2022-07-29 | Ichnos Sciences SA | Production of t cell retargeting hetero-dimeric immunoglobulins |
| WO2015095412A1 (fr) | 2013-12-19 | 2015-06-25 | Zhong Wang | Anticorps bispécifique comprenant deux fragments de liaison à l'antigène à domaine unique |
| WO2015121383A1 (fr) | 2014-02-12 | 2015-08-20 | Michael Uhlin | Anticorps bispécifiques utilisables dans une transplantation de cellules souches |
| TWI754319B (zh) | 2014-03-19 | 2022-02-01 | 美商再生元醫藥公司 | 用於腫瘤治療之方法及抗體組成物 |
| UA119167C2 (uk) | 2014-03-28 | 2019-05-10 | Зенкор, Інк. | Біспецифічне антитіло, яке зв'язується з cd38 та cd3 |
| MX2017001011A (es) * | 2014-07-21 | 2018-05-28 | Novartis Ag | Tratamiento de cancer de usando un receptor quimerico de antigeno anti-bcma. |
| EP3172235A2 (fr) | 2014-07-25 | 2017-05-31 | Cytomx Therapeutics Inc. | Anticorps anti-cd3, anticorps anti-cd3 activables, anticorps anti-cd3 multispécifiques, anticorps anti-cd3 activables multispécifiques et procédés d'utilisation de ces anticorps |
| PT3209698T (pt) | 2014-10-22 | 2018-12-14 | Crescendo Biologics Ltd | Ratinhos transgénicos |
| EP3023437A1 (fr) | 2014-11-20 | 2016-05-25 | EngMab AG | Anticorps bispécifiques contre la CD3epsilon et BCMA |
| PT3221357T (pt) | 2014-11-20 | 2020-07-28 | Hoffmann La Roche | Cadeias leves comuns e métodos de utilização |
| BR112017012502B1 (pt) | 2014-12-12 | 2020-09-15 | Bluebird Bio, Inc. | Polinucleotídeo, polipeptídeo de car codificado pelo dito polinucleotídeo, vetor compreendendo o dito polinucleotídeo, composição compreendendo o dito vetor e método para geração de uma célula imune efetora compreendendo um car |
| GB201500461D0 (en) | 2015-01-12 | 2015-02-25 | Cresendo Biolog Ltd | Therapeutic molecules |
| AU2016264725B2 (en) | 2015-05-20 | 2021-05-27 | Janssen Biotech, Inc. | Anti-CD38 antibodies for treatment of light chain amyloidosis and other CD38-positive hematological malignancies |
| CN105384825B (zh) | 2015-08-11 | 2018-06-01 | 南京传奇生物科技有限公司 | 一种基于单域抗体的双特异性嵌合抗原受体及其应用 |
| MX2018002043A (es) * | 2015-08-17 | 2018-07-06 | Janssen Pharmaceutica Nv | ANTICUERPOS ANTI-BCMA, MOLíCULAS DE UNIíN A ANTíGENOS BIESPECíFICAS QUE SE UNEN A BCMA Y CD3, Y USOS DE ESTOS. |
| US10865249B2 (en) | 2015-11-10 | 2020-12-15 | University Medical Center Hamburg-Eppendorf | Antigen-binding polypeptides directed against CD38 |
| CA3029209A1 (fr) * | 2016-06-21 | 2017-12-28 | Teneobio, Inc. | Anticorps se liant a cd3 |
| AU2017316604A1 (en) | 2016-08-24 | 2019-04-11 | Teneobio, Inc. | Transgenic non-human animals producing modified heavy chain-only antibodies |
| BR112019004873A2 (pt) | 2016-09-14 | 2019-06-11 | Teneobio Inc | anticorpos de ligação a cd3 |
| CN110167964B (zh) | 2016-11-02 | 2023-12-01 | 百时美施贵宝公司 | 组合用于治疗多发性骨髓瘤的针对bcma和cd3的双特异性抗体和免疫药物 |
| MX2019007379A (es) | 2016-12-21 | 2019-09-18 | Teneobio Inc | Anticuerpos anti-bcma unicamente de cadena pesada. |
| JP7240335B2 (ja) | 2017-06-20 | 2023-03-15 | テネオワン， インコーポレイテッド | 抗ｂｃｍａ重鎖のみ抗体 |
| CN117866097A (zh) | 2017-06-20 | 2024-04-12 | 特尼奥生物股份有限公司 | 仅有重链的抗bcma抗体 |
| WO2019000223A1 (fr) | 2017-06-27 | 2019-01-03 | Nanjing Legend Biotech Co., Ltd. | Activateurs de cellules effectrices immunitaires d'anticorps chimériques et leurs procédés d'utilisation |
| ES2928296T3 (es) | 2017-06-30 | 2022-11-16 | Us Health | Receptores de antígenos quiméricos anti-antígenos de maduración de linfocitos B con dominios humanos |
| EP3728319A1 (fr) | 2017-12-22 | 2020-10-28 | TeneoBio, Inc. | Anticorps à chaîne lourde se liant à cd22 |
| WO2019133761A1 (fr) | 2017-12-27 | 2019-07-04 | Teneobio, Inc. | Anticorps spécifiques de l'hétérodimère cd3-delta/epsilon |
| EP3801551A4 (fr) | 2018-05-24 | 2022-04-06 | Ayala Pharmaceuticals Inc. | Compositions comprenant des composés bisfluoroalkyl-1,4-benzodiazépinone et des agents immunothérapeutiques et leurs méthodes d'utilisation |
| JP7439046B2 (ja) | 2018-07-20 | 2024-02-27 | テネオツー・インコーポレイテッド | Ｃｄ１９に結合する重鎖抗体 |
| US20210355215A1 (en) | 2018-09-21 | 2021-11-18 | Teneobio, Inc. | Methods for purifying heterodimeric, multispecific antibodies |
| BR112021000173A2 (pt) | 2018-10-26 | 2021-05-04 | Teneobio, Inc. | anticorpos de cadeia pesada com ligação a cd38 |
| EP3947470A1 (fr) | 2019-04-05 | 2022-02-09 | TeneoBio, Inc. | Anticorps à chaîne lourde se liant à psma |
| WO2020252366A1 (fr) | 2019-06-14 | 2020-12-17 | Teneobio, Inc. | Anticorps à chaînes lourdes multispécifiques se liant à cd22 et cd3 |
| EP4077391A1 (fr) | 2019-12-18 | 2022-10-26 | Teneofour, Inc. | Anticorps à chaîne lourde se liant à cd38 |
| WO2021222578A1 (fr) | 2020-04-29 | 2021-11-04 | Teneobio, Inc. | Anticorps à chaîne lourde multispécifiques ayant des régions constantes de chaîne lourde modifiées |
| US20210403587A1 (en) | 2020-04-29 | 2021-12-30 | Teneobio, Inc. | Methods of treating multiple myeloma |
| US20230203161A1 (en) | 2020-04-29 | 2023-06-29 | Teneobio, Inc | Multispecific heavy chain antibodies with modified heavy chain constant regions |
| EP4171750A1 (fr) | 2020-06-30 | 2023-05-03 | Teneobio, Inc. | Anticorps multi-spécifiques se liant à bcma |
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| US11427642B2 (en) | 2022-08-30 |
| JP2020524000A (ja) | 2020-08-13 |
| CN110945026B (zh) | 2024-03-19 |
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| JP2023071876A (ja) | 2023-05-23 |
| CN117567624A (zh) | 2024-02-20 |
| EP3642236A1 (fr) | 2020-04-29 |
| MX2019015563A (es) | 2020-07-28 |
| JP7240335B2 (ja) | 2023-03-15 |
| AU2018288803A1 (en) | 2020-02-06 |
| US20200157232A1 (en) | 2020-05-21 |
| US20230060847A1 (en) | 2023-03-02 |
| CN110945026A (zh) | 2020-03-31 |
| WO2018237006A1 (fr) | 2018-12-27 |
| JP7465382B2 (ja) | 2024-04-10 |
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